Chlorpromazine hydrochloride

Generic: Chlorpromazine hydrochloride

Labeler: Major Pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive

Drug Facts

Product Profile

Brand Name Chlorpromazine hydrochloride
Generic Name Chlorpromazine hydrochloride
Labeler Major Pharmaceuticals
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

CHLORPROMAZINE HYDROCHLORIDE 50 mg/1

Identifiers & Regulatory

Product NDC 0904-7131
Product ID 0904-7131_5f66c7a0-171c-4cc8-8160-99a7b89ea527
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213368
Marketing Start 2020-01-27
Marketing End 2026-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09047131
Hyphenated Format 0904-7131

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name Chlorpromazine hydrochloride (source: ndc)
Generic Name Chlorpromazine hydrochloride (source: ndc)
Application Number ANDA213368 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (0904-7131-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (1)

0904-7131-61 100 BLISTER PACK in 1 CARTON (0904-7131-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (1)

CHLORPROMAZINE HYDROCHLORIDE (50 mg/1)

Linked Drug Pages (1)

Chlorpromazine hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5f66c7a0-171c-4cc8-8160-99a7b89ea527", "openfda": {"unii": ["9WP59609J6"], "rxcui": ["991039", "991044", "991188", "991194", "991336"], "spl_set_id": ["d58570a0-58b0-4662-b2ad-aa8d1463b4c1"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7131-61)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-7131-61", "marketing_end_date": "20260228", "marketing_start_date": "20200127"}], "brand_name": "Chlorpromazine hydrochloride", "product_id": "0904-7131_5f66c7a0-171c-4cc8-8160-99a7b89ea527", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0904-7131", "generic_name": "Chlorpromazine hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA213368", "marketing_category": "ANDA", "marketing_end_date": "20260228", "marketing_start_date": "20200127"}